Driven by a passion for helping patients, Duke-NUS Medical School alumna combines over a decade of clinical expertise in ...

Using regression analysis, the investigators found that the control of axial growth with ortho-K treatment was better in the summer than in the winter (β=-0.05; P <.001). They observed a similar ...

Zeiss Medical Technology announced today that it received FDA 510(k) clearance for the Intrabeam 700 platform.

The FDA has granted 501(k) clearance to ZEISS INTRABEAM 700, a robotic-assisted platform designed to enhance intraoperative ...

The U.S. FDA has cleared regenerative medicine company Orthocell Ltd.’s 510(k) for its nerve repair product, Remplir, paving the way to begin commercial operations in the $1.6 billion U.S. nerve ...

HighLife announced that it received FDA breakthrough device designation for its trans-septal mitral valve replacement (TMVR) solution. Paris-based HighLife — which has facilities in Irvine ...